Recall events
/
Event 92049
Event summary
Timeline bucket April 17, 2023
Product types Device
Classifications Class I
Statuses Terminated
Recalling firm wording Draeger Medical, Inc.
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
22 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 22
Seattle PAP Plus, MP02260
Z-1439-2023
Recall number Z-1439-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 32,050 untis
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1439-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[21871]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675548904; All lots distributed prior to 03/20/2023 (lots other than 0367.2702.13).
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37156]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 22
VentStar Basic (P)180, MP00351
Z-1440-2023
Recall number Z-1440-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 325 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1440-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52127]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675422068; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37226]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 22
VentStar Basic (P)250, MP00352
Z-1441-2023
Recall number Z-1441-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 200 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1441-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52124]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675422051; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37167]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 22
VentStar Watertrap (P) 180, MP00361
Z-1442-2023
Recall number Z-1442-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 50 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1442-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17070]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675422013; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37636]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 22
VentStar Watertrap (P) 180 w/oLL, MP00362
Z-1443-2023
Recall number Z-1443-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 25 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1443-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57366]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675422006; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37548]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 22
VentStar Anesthesia WT (P)180, MP00374
Z-1444-2023
Recall number Z-1444-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 130 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1444-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4333]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675421948; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37162]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 22
VentStar breathing bag Set (P) 110, MP00384
Z-1445-2023
Recall number Z-1445-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 25 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1445-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52123]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675421870; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37414]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 22
ID Circuit Basic (P) 180, MP01340
Z-1446-2023
Recall number Z-1446-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 25 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1446-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52126]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675421870; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37408]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 22
VentStar Anesthesia (N) 180, MP00333
Z-1447-2023
Recall number Z-1447-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1447-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17074]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675422198; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37545]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1448-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 1,725 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1448-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9691]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 40048675422044; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37410]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1449-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 125 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1449-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40474]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675421993; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[5082]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1450-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 375 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1450-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17072]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675421887; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[5087]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1451-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 280 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1451-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4329]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675421917; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37643]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1452-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 200,900 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1452-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46173]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675412014; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37685]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1453-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 329,294 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1453-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52128]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675412038; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37681]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1454-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 2,380 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1454-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28138]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675545552; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37639]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1455-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 18,160 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1455-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9683]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675545576; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[4842]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1456-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1456-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40477]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675545590; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37205]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1457-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 40 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1457-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28140]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Compare all device evidence states
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Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675545613; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37174]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1458-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1458-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57369]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675552833; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[5077]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1459-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 500 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1459-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46175]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675544739; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37149]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1460-2023
Initiated April 17, 2023
Classification Class I
Status Terminated
Quantity 720 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1460-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33824]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Code information UDI-DI: 04048675695622; All lots.
Distribution pattern Domestic: US Nationwide Distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[4849]
FDA event record
· Exact recall-number query on openFDA
